- IQVIA (Carlsbad, CA)
- …Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and ... phases as required. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) per GCP/ICH and local… more
- IQVIA (Carlsbad, CA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- IQVIA (Carlsbad, CA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... IQVIA Biotech is hiring for our Early Clinical Development team. Ideal candidates will have Phase...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- Bristol Myers Squibb (San Diego, CA)
- …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... we pioneer. Join us and make a difference. The Senior Manager, Clinical Data Management (Data Management...BMS R&D pipeline. This role reports to the Director, Clinical Data Management or Associate Director, … more
- Edwards Lifesciences (San Diego, CA)
- …the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead + FDA/EMEA/PMDA submission experience + The ... + Act as core team member/lead biostatistician of assigned clinical trial (s) in US and international/global ...prevention of pollution under their span of influence/control The Sr Manager, Biostatistics Level is lateral to Associate… more